1. Assembly defects induce oxidative stress in inherited mitochondrial complex I deficiency. (August 2015) Authors: Leman, Géraldine; Gueguen, Naïg; Desquiret-Dumas, Valérie; Kane, Mariame Selma; Wettervald, Céline; Chupin, Stéphanie; Chevrollier, Arnaud; Lebre, Anne-Sophie; Bonnefont, Jean-Paul; Barth, Magalie; Amati-Bonneau, Patrizia; Verny, Christophe; Henrion, Daniel; Bonneau, Dominique; Reynier, Pascal; P... Journal: International journal of biochemistry & cell biology Issue: Volume 65(2015:Aug.) Page Start: 91 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. CBMT-11. HIGH MITOCHONDRIAL DNA COPY NUMBER IS ASSOCIATED WITH LONGER SURVIVAL IN YOUNG PATIENTS WITH GLIOBLASTOMA. (11th November 2019) Authors: Rousseau, Audrey; Dardaud, Laure-Marie; Bris, Céline; Desquiret-Dumas, Valérie; Boisselier, Blandine; Tabouret, Emeline; Mokhtari, Karima; Figarella-Branger, Dominique; Procaccio, Vincent Journal: Neuro-oncology Issue: Volume 21(2019)Supplement 6 Page Start: vi35 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. High mitochondrial DNA copy number is associated with longer survival in young patients with glioblastoma. Issue 8 (26th April 2019) Authors: Dardaud, Laure-Marie; Bris, Céline; Desquiret-Dumas, Valérie; Boisselier, Blandine; Tabouret, Emeline; Mokhtari, Karima; Figarella-Branger, Dominique; Rousseau, Audrey; Procaccio, Vincent Journal: Neuro-oncology Issue: Volume 21:Issue 8(2019) Page Start: 1084 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Mitochondrial DNA copy number as a prognostic marker is age-dependent in adult glioblastoma. Issue 1 (3rd January 2022) Authors: Sourty, Baptiste; Dardaud, Laure-Marie; Bris, Céline; Desquiret-Dumas, Valérie; Boisselier, Blandine; Basset, Laëtitia; Figarella-Branger, Dominique; Morel, Alain; Sanson, Marc; Procaccio, Vincent; Rousseau, Audrey Journal: Neuro-oncology advances Issue: Volume 4:Issue 1(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy. (June 2020) Authors: Charif, Majida; Chevrollier, Arnaud; Gueguen, Naïg; Bris, Céline; Goudenège, David; Desquiret-Dumas, Valérie; Leruez, Stéphanie; Colin, Estelle; Meunier, Audrey; Vignal, Catherine; Smirnov, Vasily; Defoort-Dhellemmes, Sabine; Drumare Bouvet, Isabelle; Goizet, Cyril; Votruba, Marcela; Jurkute, Ner... Journal: Neurology Issue: Volume 6:Number 3(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders. Issue 10 (11th July 2013) Authors: Bannwarth, Sylvie; Procaccio, Vincent; Lebre, Anne Sophie; Jardel, Claude; Chaussenot, Annabelle; Hoarau, Claire; Maoulida, Hassani; Charrier, Nathanaël; Gai, Xiaowu; Xie, Hongbo M; Ferre, Marc; Fragaki, Konstantina; Hardy, Gaëlle; Mousson de Camaret, Bénédicte; Marlin, Sandrine; Dhaenens, Claire... Journal: Journal of medical genetics Issue: Volume 50:Issue 10(2013) Page Start: 704 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Study of mitochondrial function in placental insufficiency. (July 2018) Authors: Lefebvre, Tiphaine; Roche, Ombeline; Seegers, Valérie; Cherif, Majida; Khiati, Salim; Gueguen, Naïg; Desquiret-Dumas, Valérie; Geffroy, Guillaume; Blanchet, Odile; Reynier, Pascal; Legendre, Guillaume; Lenaers, Guy; Procaccio, Vincent; Gascoin, Géraldine Journal: Placenta Issue: Volume 67(2018) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗